Pages that link to "Q35939147"

The following pages link to Identification of multiple quantitative trait loci linked to prion disease incubation period in mice (Q35939147):

Displaying 50 items.

• Selective incorporation of polyanionic molecules into hamster prions (Q24596538) (← links)
• A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea (Q24642582) (← links)
• Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice (Q24651920) (← links)
• A systems approach to prion disease (Q24656032) (← links)
• Formation of native prions from minimal components in vitro (Q24676353) (← links)
• The state of the prion (Q28288758) (← links)
• Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1. (Q28363814) (← links)
• Correlation analysis for the incubation period of prion disease (Q28729089) (← links)
• Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP (Q28943533) (← links)
• Identification of a gene regulatory network associated with prion replication (Q30458186) (← links)
• Early behavioral changes and quantitative analysis of neuropathological features in murine prion disease: stereological analysis in the albino Swiss mice model (Q30466255) (← links)
• Cathepsin D SNP associated with increased risk of variant Creutzfeldt-Jakob disease (Q33329713) (← links)
• HECTD2 is associated with susceptibility to mouse and human prion disease (Q33408776) (← links)
• Conversion efficiency of bank vole prion protein in vitro is determined by residues 155 and 170, but does not correlate with the high susceptibility of bank voles to sheep scrapie in vivo (Q33449340) (← links)
• HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10q. (Q33503386) (← links)
• The retinoic acid receptor beta (Rarb) region of Mmu14 is associated with prion disease incubation time in mouse (Q33769410) (← links)
• Evidence for varied aetiologies regulating the transmission of prion disease: implications for understanding the heritable basis of prion incubation times (Q33769832) (← links)
• A polymorphism in the regulatory region of PRNP is associated with increased risk of sporadic Creutzfeldt-Jakob disease (Q33907233) (← links)
• Gene expression profiling and association with prion-related lesions in the medulla oblongata of symptomatic natural scrapie animals (Q33918266) (← links)
• The first report of RPSA polymorphisms, also called 37/67 kDa LRP/LR gene, in sporadic Creutzfeldt-Jakob disease (CJD). (Q33992073) (← links)
• Kuru in the 21st century--an acquired human prion disease with very long incubation periods (Q33997105) (← links)
• Spontaneous generation of mammalian prions (Q34069434) (← links)
• Sex effects in mouse prion disease incubation time (Q34103332) (← links)
• Molecular pathology of human prion disease (Q34462913) (← links)
• Review: contribution of transgenic models to understanding human prion disease. (Q34474868) (← links)
• Sod1 deficiency reduces incubation time in mouse models of prion disease (Q34563121) (← links)
• The epidemiology of variant Creutzfeldt-Jakob disease in Europe (Q34574513) (← links)
• Detection of new quantitative trait Loci for susceptibility to transmissible spongiform encephalopathies in mice (Q34619306) (← links)
• The role of the NADPH oxidase NOX2 in prion pathogenesis (Q34682177) (← links)
• Influence of the prion protein gene, Prnp, on scrapie susceptibility in sheep (Q34685443) (← links)
• Species-barrier-independent prion replication in apparently resistant species. (Q34685449) (← links)
• Mammalian prion proteins: enigma, variation and vaccination (Q34691392) (← links)
• Mouse models of prion disease transmission (Q34970614) (← links)
• Transgenesis applied to transmissible spongiform encephalopathies (Q35037396) (← links)
• In vitro conversion of normal prion protein into pathologic isoforms (Q35122360) (← links)
• Microglial Cx3cr1 knockout reduces prion disease incubation time in mice (Q35127326) (← links)
• Molecular neurology of prion disease (Q35488760) (← links)
• Molecular and clinical classification of human prion disease (Q35549016) (← links)
• Genome wide association studies and prion disease (Q35578768) (← links)
• Rational targeting for prion therapeutics. (Q35990277) (← links)
• Genomic Characteristics of Genetic Creutzfeldt-Jakob Disease Patients with V180I Mutation and Associations with Other Neurodegenerative Disorders (Q36060992) (← links)
• Human and animal spongiform encephalopathies are autoimmune diseases: a novel theory and its supporting evidence (Q36083479) (← links)
• In vitro amplification of scrapie and chronic wasting disease PrP(res) using baculovirus-expressed recombinant PrP as substrate (Q36147244) (← links)
• Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in mice (Q36187263) (← links)
• Phenotypic variability in human prion diseases. (Q36310865) (← links)
• The risk of transmission of variant Creutzfeldt-Jakob disease via contact lenses and ophthalmic devices (Q36319802) (← links)
• Prion diseases of humans and farm animals: epidemiology, genetics, and pathogenesis (Q36521947) (← links)
• The infectivity of transmissible spongiform encephalopathy agent at low doses: the importance of phospholipid (Q36553818) (← links)
• A critical analysis of disease-associated DNA polymorphisms in the genes of cattle, goat, sheep, and pig. (Q36571037) (← links)
• Mouse prion protein polymorphism Phe-108/Val-189 affects the kinetics of fibril formation and the response to seeding: evidence for a two-step nucleation polymerization mechanism (Q36620764) (← links)